PREPARATION AND RELEASE CHARACTERISTICS OF POLYMER-REINFORCED AND COATED ALGINATE BEADS

被引:16
作者
LEE, BJ [1 ]
MIN, GH [1 ]
机构
[1] KANGWEON NATL UNIV,COLL PHARM,CHUNCHON 200701,SOUTH KOREA
关键词
ALGINATE BEADS; MATRICES; POLYMERIC-REINFORCED; EUDRAGIT(R) RS100; COATING; PLASTICIZER; RELEASE RATE; SWELLING; EROSION;
D O I
10.1007/BF02979193
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Polymeric reinforcement and coatings of alginate beads were carried out to control the release rate of drug from alginate beads. A poorly water-soluble ibuprofen (IPF) was selected as a model drug. A commercially available Eudragit(R) RS100 was also used as a polymer. Effects of polymeric contents, the presence of plasticizers and amount of drug loading on the release rate of drug were investigated. The release rate of drug from alginate beads in the simulated gastric fluid did not occur within 2 h but released immediately when dissolution media were switched to the simulated intestinal fluid. No significant difference of release rate from polymer-reinforced alginate bead without plasticizers was observed when compared to plain (simple) beads. However, the release rate of drug from polymer-reinforced alginate beads was further sustained and retarded when aluminium tristearate (AT) as a plasticizer was added to polymer. However, polyethylene glycol 400 (PEG400) did not change the release rate of drug from alginate beads although PEC400 was used to improve dispersion of polymer and sodium alginate, and plasticize Eudragit(R) RS100 polymer. The presence of plasticizer was crucial to reinforce alginate gel matrices using a polymer. As the amount of drug loading increased, the release rate of drug increased as a result of decreasing effects of polymer contents in matrices. The significantly sustained release of drug from polymer-coated alginate beads occurred as the amount of polymer increased because the thickness of coated membrane increased so that cracks and pores of the outer surface of alginate beads could be reduced. The sustained and retarded action of polymer-reinforced and coated beads may result from the disturbance of swelling and erosion (disintegration) of alginate beads. From these findings, polymeric-reinforcement and coatings of alginate gel beads can provide an advanced delivery system by retarding the release I ate of various drugs.
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收藏
页码:183 / 188
页数:6
相关论文
共 15 条
[1]   SPHERICAL AGGLOMERATES OF WATER-INSOLUBLE DRUGS [J].
BODMEIER, R ;
PAERATAKUL, O .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1989, 78 (11) :964-967
[2]   QUANTITATIVE DETERMINATION OF URONIC ACID COMPOSITION OF ALGINATES [J].
HAUG, A ;
LARSEN, B .
ACTA CHEMICA SCANDINAVICA, 1962, 16 (08) :1908-&
[3]   DEGRADATION OF ALGINATES AT DIFFERENT PH VALUES [J].
HAUG, A ;
SMIDSROD, O ;
LARSEN, B .
ACTA CHEMICA SCANDINAVICA, 1963, 17 (05) :1466-&
[4]  
HWANG SJ, 1993, J KOR PHARM SCI, V23, P19
[5]  
KAWATA M, 1986, CHEM PHARM BULL, V34, P2613
[6]   THE CONTROLLED RELEASE OF BLUE DEXTRAN FROM ALGINATE BEADS [J].
KIM, CK ;
LEE, EJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1992, 79 (01) :11-19
[7]  
KOJI D, 1981, YAKUGAKU ZASSHI, V101, P452
[8]  
Lee Beom-Jin, 1995, Archives of Pharmacal Research (Seoul), V18, P22, DOI 10.1007/BF02976502
[9]  
Lehmann K., 1989, AQUEOUS POLYM COATIN, P153
[10]  
LIN S, 1992, PHARMACEUT RES, P1128